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Effect of methadone and acepromazine premedication on tear production in dogs

OBJECTIVES: To evaluate the combined effect of intramuscular acepromazine and methadone on tear production in dogs undergoing general anaesthesia for elective, non-ocular procedures. DESIGN: Prospective, non-randomised, pre-post treatment study. SETTING: Patients were recruited from a referral pract...

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Autores principales: Volk, Hayley A, West, Ellie, Linn-Pearl, Rose Non, Fricker, Georgina V, Panti, Ambra, Gould, David J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307564/
https://www.ncbi.nlm.nih.gov/pubmed/30613403
http://dx.doi.org/10.1136/vetreco-2018-000298
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author Volk, Hayley A
West, Ellie
Linn-Pearl, Rose Non
Fricker, Georgina V
Panti, Ambra
Gould, David J
author_facet Volk, Hayley A
West, Ellie
Linn-Pearl, Rose Non
Fricker, Georgina V
Panti, Ambra
Gould, David J
author_sort Volk, Hayley A
collection PubMed
description OBJECTIVES: To evaluate the combined effect of intramuscular acepromazine and methadone on tear production in dogs undergoing general anaesthesia for elective, non-ocular procedures. DESIGN: Prospective, non-randomised, pre-post treatment study. SETTING: Patients were recruited from a referral practice in the UK. METHODS: Thirty client-owned dogs were enrolled in this study and received a combined intramuscular premedication of methadone (0.3 mg/kg) and acepromazine (0.02 mg/kg) before general anaesthesia for elective, non-ocular procedures. Full ophthalmic examination was performed and tear production was quantified using the Schirmer tear test-1 (STT-1). On the day of general anaesthesia, an STT-1 was performed before (STT-1a) and after (STT-1b) intramuscular premedication with methadone/acepromazine. RESULTS: Using a general linear model, a significant effect on STT-1 results was found for premedication with methadone/acepromazine (P=0.013), but not eye laterality (P=0.527). Following premedication, there was a significant reduction observed in the mean STT-1 readings of left and right eyes between STT-1a (20.4±2.8 mm/min) and STT-1b (16.9±4.1 mm/min; P<0.001). Significantly more dogs had an STT-1 reading less than 15 mm/min in one or both eyes after premedication (30 per cent; 9/30 dogs) compared with before premedication (6.7 per cent; 2/30 dogs; P=0.042). CONCLUSIONS: An intramuscular premedication of methadone and acepromazine results in a decrease in tear production in dogs before elective general anaesthesia. This may contribute to the risk of ocular morbidities, such as corneal ulceration, particularly in patients with lower baseline tear production.
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spelling pubmed-63075642019-01-04 Effect of methadone and acepromazine premedication on tear production in dogs Volk, Hayley A West, Ellie Linn-Pearl, Rose Non Fricker, Georgina V Panti, Ambra Gould, David J Vet Rec Open Companion or Pet Animals OBJECTIVES: To evaluate the combined effect of intramuscular acepromazine and methadone on tear production in dogs undergoing general anaesthesia for elective, non-ocular procedures. DESIGN: Prospective, non-randomised, pre-post treatment study. SETTING: Patients were recruited from a referral practice in the UK. METHODS: Thirty client-owned dogs were enrolled in this study and received a combined intramuscular premedication of methadone (0.3 mg/kg) and acepromazine (0.02 mg/kg) before general anaesthesia for elective, non-ocular procedures. Full ophthalmic examination was performed and tear production was quantified using the Schirmer tear test-1 (STT-1). On the day of general anaesthesia, an STT-1 was performed before (STT-1a) and after (STT-1b) intramuscular premedication with methadone/acepromazine. RESULTS: Using a general linear model, a significant effect on STT-1 results was found for premedication with methadone/acepromazine (P=0.013), but not eye laterality (P=0.527). Following premedication, there was a significant reduction observed in the mean STT-1 readings of left and right eyes between STT-1a (20.4±2.8 mm/min) and STT-1b (16.9±4.1 mm/min; P<0.001). Significantly more dogs had an STT-1 reading less than 15 mm/min in one or both eyes after premedication (30 per cent; 9/30 dogs) compared with before premedication (6.7 per cent; 2/30 dogs; P=0.042). CONCLUSIONS: An intramuscular premedication of methadone and acepromazine results in a decrease in tear production in dogs before elective general anaesthesia. This may contribute to the risk of ocular morbidities, such as corneal ulceration, particularly in patients with lower baseline tear production. BMJ Publishing Group 2018-12-05 /pmc/articles/PMC6307564/ /pubmed/30613403 http://dx.doi.org/10.1136/vetreco-2018-000298 Text en © British Veterinary Association 2018. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Companion or Pet Animals
Volk, Hayley A
West, Ellie
Linn-Pearl, Rose Non
Fricker, Georgina V
Panti, Ambra
Gould, David J
Effect of methadone and acepromazine premedication on tear production in dogs
title Effect of methadone and acepromazine premedication on tear production in dogs
title_full Effect of methadone and acepromazine premedication on tear production in dogs
title_fullStr Effect of methadone and acepromazine premedication on tear production in dogs
title_full_unstemmed Effect of methadone and acepromazine premedication on tear production in dogs
title_short Effect of methadone and acepromazine premedication on tear production in dogs
title_sort effect of methadone and acepromazine premedication on tear production in dogs
topic Companion or Pet Animals
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6307564/
https://www.ncbi.nlm.nih.gov/pubmed/30613403
http://dx.doi.org/10.1136/vetreco-2018-000298
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